Literature DB >> 8513332

Dystrophin expression in the human retina is required for normal function as defined by electroretinography.

D A Pillers1, D E Bulman, R G Weleber, D A Sigesmund, M A Musarella, B R Powell, W H Murphey, C Westall, C Panton, L E Becker.   

Abstract

We have studied retinal function by electroretinography in five Becker and six Duchenne muscular dystrophy patients. All had abnormal electroretinograms with a markedly reduced amplitude for the b-wave in the dark-adapted state. Using three antisera raised to different domains of dystrophin, we identified dystrophin in the outer plexiform layer of human retina. The retinal dystrophin is present in multiple isoforms as the result of alternative splicing. The localization of dystrophin to the outer plexiform layer coincident with the abnormal b-wave suggests that dystrophin is required for normal retinal electrophysiology.

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Year:  1993        PMID: 8513332     DOI: 10.1038/ng0593-82

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  38 in total

1.  ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy.

Authors:  K M Fitzgerald; G W Cibis; A H Gettel; R Rinaldi; D J Harris; R A White
Journal:  J Med Genet       Date:  1999-04       Impact factor: 6.318

Review 2.  The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease.

Authors:  Kirill A Martemyanov; Alapakkam P Sampath
Journal:  Annu Rev Vis Sci       Date:  2017-07-17       Impact factor: 6.422

3.  Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exons.

Authors:  Zhujun Zhang; Yasuaki Habara; Atsushi Nishiyama; Yoshinobu Oyazato; Mariko Yagi; Yasuhiro Takeshima; Masafumi Matsuo
Journal:  J Hum Genet       Date:  2007-06-20       Impact factor: 3.172

Review 4.  Mechanisms of resistance to pathogenesis in muscular dystrophies.

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1999-05       Impact factor: 3.396

Review 5.  Emerging Strategies in the Treatment of Duchenne Muscular Dystrophy.

Authors:  Perry B Shieh
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

6.  Pikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpression.

Authors:  Huaiyu Hu; Jing Li; Zhen Zhang; Miao Yu
Journal:  Neurosci Lett       Date:  2010-12-01       Impact factor: 3.046

7.  Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway.

Authors:  K M Fitzgerald; G W Cibis; S A Giambrone; D J Harris
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

8.  Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat.

Authors:  Sabrina V Böhm; Panayiotis Constantinou; Sipin Tan; Hong Jin; Roland G Roberts
Journal:  BMC Biol       Date:  2009-12-04       Impact factor: 7.431

9.  Adeno-associated virus serotype-9 efficiently transduces the retinal outer plexiform layer.

Authors:  Bo Lei; Keqing Zhang; Yongping Yue; Arkasubhra Ghosh; Dongsheng Duan
Journal:  Mol Vis       Date:  2009-07-17       Impact factor: 2.367

Review 10.  The roles of the dystrophin-associated glycoprotein complex at the synapse.

Authors:  Gonneke S K Pilgram; Saranyapin Potikanond; Richard A Baines; Lee G Fradkin; Jasprina N Noordermeer
Journal:  Mol Neurobiol       Date:  2009-11-09       Impact factor: 5.590

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